Honing Judith, Pavlov Kirill V, Meijer Coby, Smit Justin K, Boersma-van Ek Wytske, Karrenbeld Arend, Burgerhof Johannes G M, Kruyt Frank A E, Plukker John Th M
Department of Surgery, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands,
Ann Surg Oncol. 2014 Dec;21 Suppl 4:S657-64. doi: 10.1245/s10434-014-3763-x. Epub 2014 May 16.
It has been suggested that markers associated with cancer stem cells (CSC) may play a role in esophageal cancer. Our aim was to investigate the expression pattern of proposed CSC markers ALDH1, Axin2, BMI1, CD44, and SOX2 in esophageal adenocarcinoma (EAC) and to relate their expression to survival.
In this study we included 94 EAC patients and examined the expression of the above-mentioned markers by using immunohistochemistry on tissue microarrays. Expression was scored as positive or negative or categorized as low or high in terms of an immunoreactivity score (IRS). Expression rates were related to clinicopathologic characteristics and overall and disease-free survival (DFS).
In a multivariate analysis, negative expression of CD44 and of SOX2 were both significant prognostic factors for DFS [hazard ratio (HR), 1.73; 95 % confidence interval (CI), 1.00-2.96; P = 0.046 and HR, 2.06; 95 % CI 1.14-3.70 P = 0.016). When CD44 and SOX2 expression were analyzed together, negative SOX2 expression was an independent prognostic factor for DFS (HR, 1.91; 95 % CI 1.05-3.46; P = 0.034). Low IRS scores for ALDH1 or Axin2 were associated with a reduced median survival (12.8 vs. 28.7 and 12.1 vs. 25.5 months, respectively). However, these markers and BMI1 were not prognostic factors for survival.
Loss of CD44 expression and loss of SOX2 expression are prognostic factors of poor survival in EAC patients. This suggests a role of these proteins in EAC that requires further investigation.
有研究表明,与癌症干细胞(CSC)相关的标志物可能在食管癌中发挥作用。我们的目的是研究食管癌(EAC)中公认的癌症干细胞标志物醛脱氢酶1(ALDH1)、轴抑制蛋白2(Axin2)、多梳蛋白抑制复合物2亚基BMI1(BMI1)、细胞表面分化抗原44(CD44)和性别决定区Y框蛋白2(SOX2)的表达模式,并将它们的表达与生存率相关联。
在本研究中,我们纳入了94例EAC患者,并通过组织芯片免疫组化检测上述标志物的表达。根据免疫反应评分(IRS),将表达分为阳性或阴性,或分为低表达或高表达。表达率与临床病理特征、总生存期和无病生存期(DFS)相关。
在多变量分析中,CD44和SOX2的阴性表达均为DFS的显著预后因素[风险比(HR),1.73;95%置信区间(CI),1.00 - 2.96;P = 0.046和HR,2.06;95% CI 1.14 - 3.70,P = 0.016]。当一起分析CD44和SOX2表达时,SOX2阴性表达是DFS的独立预后因素(HR,1.91;95% CI 1.05 - 3.46;P = 0.034)。ALDH1或Axin2的低IRS评分与中位生存期缩短相关(分别为12.8个月对28.7个月和12.1个月对25.5个月)。然而,这些标志物和BMI1不是生存的预后因素。
CD44表达缺失和SOX2表达缺失是EAC患者生存不良的预后因素。这表明这些蛋白在EAC中发挥作用,需要进一步研究。